Genopathy
Gene-Disorder Association · Article
Gene
CPLX1
Complexin 1
Disorder
Myoclonic Epilepsy, Familial Infantile
First reported 1968
Supporting publications 1
Key publication · disorder Familial infantile myoclonic epilepsy in a family suffering from tuberous sclerosis.Epilepsia · 1968
Manually curated
Association Review

In brief

The association between CPLX1 (Complexin 1) and Myoclonic Epilepsy, Familial Infantile is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.

Sources 2
Clinical variants 0
Symptoms 45
Compounds 0
Trials 0
Publications 1
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

2 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
CPLX1

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Myoclonic Epilepsy, Familial Infantile

The disorder

7 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

31 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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07
Literature

Reading

1 publication

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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08
Provenance

References & sources

7 references

Every source and publication cited across this dossier, as one numbered reference list.

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